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Study of the Efficacy of Lurasidone in Cognitive Functioning in Bipolar Patients — ELICE_BD  

Bipolar Disorder Clinical Trial

Official title:
A 6-Week Randomised, Double-Blind, Placebo-Controlled, Multicenter Study to Evaluate the Efficacy of Lurasidone Adjunctive Therapy in Improving Cognitive Functioning in Euthymic Bipolar Disorder Patients (ELICE-BD)

Clinical Trial Summary

This is a randomized, double-blind, placebo-controlled, multicentre, parallel-group study to assess the cognitive effects of lurasidone in bipolar I and II patients (manic depression) who are in remission from an episode. Participants who show cognitive impairment at the screening visit will be enrolled into the study and randomized at the baseline visit to receive either lurasidone or placebo adjunctive therapy in a 1:1 ratio for 6 weeks.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02731612
Study type Interventional
Source University of British Columbia
Contact Nazlin Walji, B.Sc
Phone 604-822-7294
Email nazlin.walji@ubc.ca
Status Recruiting
Phase Phase 3
Start date May 8, 2017
Completion date March 31, 2025
View Details
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